Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey MO Chandesris, I Melki, A Natividad, A Puel, C Fieschi, L Yun, ... Medicine 91 (4), e1-e19, 2012 | 337 | 2012 |
BRAF mutation correlates with high-risk Langerhans cell histiocytosis and increased resistance to first-line therapy S Héritier, JF Emile, MA Barkaoui, C Thomas, S Fraitag, S Boudjemaa, ... Journal of clinical oncology 34 (25), 3023, 2016 | 314 | 2016 |
Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies A Fischer, J Provot, JP Jais, A Alcais, N Mahlaoui, D Adoue, N Aladjidi, ... Journal of Allergy and Clinical Immunology 140 (5), 1388-1393. e8, 2017 | 306 | 2017 |
New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children N Aladjidi, G Leverger, T Leblanc, MQ Picat, G Michel, Y Bertrand, ... haematologica 96 (5), 655, 2011 | 252 | 2011 |
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation B Neven, A Magerus-Chatinet, B Florkin, D Gobert, O Lambotte, ... Blood, The Journal of the American Society of Hematology 118 (18), 4798-4807, 2011 | 180 | 2011 |
Vemurafenib for refractory multisystem Langerhans cell histiocytosis in children: an international observational study J Donadieu, IA Larabi, M Tardieu, J Visser, C Hutter, E Sieni, N Kabbara, ... Journal of Clinical Oncology 37 (31), 2857, 2019 | 170 | 2019 |
Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome J Donadieu, O Fenneteau, B Beaupain, S Beaufils, F Bellanger, ... Haematologica 97 (9), 1312, 2012 | 156 | 2012 |
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype R Micol, LB Slama, F Suarez, L Le Mignot, J Beauté, N Mahlaoui, ... Journal of Allergy and Clinical Immunology 128 (2), 382-389. e1, 2011 | 154 | 2011 |
Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency J Cottineau, MC Kottemann, FP Lach, YH Kang, F Vély, EK Deenick, ... The Journal of clinical investigation 127 (5), 1991-2006, 2017 | 131 | 2017 |
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes J Hadjadj, N Aladjidi, H Fernandes, G Leverger, A Magérus-Chatinet, ... Blood, The Journal of the American Society of Hematology 134 (1), 9-21, 2019 | 125 | 2019 |
Treatment of childhood acute myeloblastic leukemia: dose intensification improves outcome and maintenance therapy is of no benefit–multicenter studies of the French LAME … Y Perel, A Auvrignon, T Leblanc, G Michel, Y Reguerre, JP Vannier, ... Leukemia 19 (12), 2082-2089, 2005 | 117 | 2005 |
Langerhans cell histiocytosis: therapeutic strategy and outcome in a 30‐year nationwide cohort of 1478 patients under 18 years of age C Rigaud, MA Barkaoui, C Thomas, Y Bertrand, A Lambilliotte, J Miron, ... British journal of haematology 174 (6), 887-898, 2016 | 114 | 2016 |
Outcome in children with relapsed acute myeloid leukemia after initial treatment with the French Leucemie Aique Myeloide Enfant (LAME) 89/91 protocol of the French Society of … N Aladjidi, A Auvrignon, T Leblanc, Y Perel, A Bénard, P Bordigoni, ... Journal of clinical oncology 21 (23), 4377-4385, 2003 | 113 | 2003 |
Brentuximab vedotin for paediatric relapsed or refractory Hodgkin's lymphoma and anaplastic large-cell lymphoma: a multicentre, open-label, phase 1/2 study F Locatelli, C Mauz-Koerholz, K Neville, A Llort, A Beishuizen, S Daw, ... The Lancet Haematology 5 (10), e450-e461, 2018 | 105 | 2018 |
Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome C Bellanné-Chantelot, B Schmaltz-Panneau, C Marty, O Fenneteau, ... Blood, The Journal of the American Society of Hematology 132 (12), 1318-1331, 2018 | 102 | 2018 |
Risk of autoimmune diseases and human papilloma virus (HPV) vaccines: Six years of case-referent surveillance L Grimaldi-Bensouda, M Rossignol, I Koné-Paut, A Krivitzky, ... Journal of Autoimmunity 79, 84-90, 2017 | 95 | 2017 |
Early-onset autoimmunity associated with SOCS1 haploinsufficiency J Hadjadj, CN Castro, M Tusseau, MC Stolzenberg, F Mazerolles, ... Nature communications 11 (1), 5341, 2020 | 89 | 2020 |
Economic evaluation of immunoglobulin replacement in patients with primary antibody deficiencies J Beaute, P Lévy, V Millet, M Debre, Y Dudoit, L Le Mignot, A Tajahmady, ... Clinical & Experimental Immunology 160 (2), 240-245, 2010 | 85 | 2010 |
Circulating cell‐free BRAFV600E as a biomarker in children with Langerhans cell histiocytosis S Héritier, Z Hélias‐Rodzewicz, H Lapillonne, N Terrones, S Garrigou, ... British journal of haematology 178 (3), 457-467, 2017 | 78 | 2017 |
Rituximab therapy for childhood Evans syndrome B Bader-Meunier, N Aladjidi, F Bellmann, F Monpoux, B Nelken, A Robert, ... haematologica 92 (12), 1691-1694, 2007 | 78 | 2007 |